class name | count |
---|---|
rosids | 34 |
asterids | 11 |
Spermatophyta | 6 |
eudicotyledons | 5 |
Liliopsida | 2 |
Magnoliophyta | 1 |
class name | count |
---|---|
Fabaceae
![]() |
27 |
Apocynaceae
![]() |
5 |
Taxaceae
![]() |
4 |
Viscaceae
![]() |
2 |
Sapotaceae
![]() |
2 |
Zingiberaceae
![]() |
1 |
Solanaceae
![]() |
1 |
Boraginaceae
![]() |
1 |
Brassicaceae
![]() |
1 |
Achariaceae
![]() |
1 |
Pinaceae
![]() |
1 |
Proteaceae
![]() |
1 |
Magnoliaceae
![]() |
1 |
Nyctaginaceae
![]() |
1 |
Euphorbiaceae
![]() |
1 |
Fagaceae
![]() |
1 |
Arecaceae
![]() |
1 |
Myrtaceae
![]() |
1 |
Cupressaceae
![]() |
1 |
Rutaceae
![]() |
1 |
br08003 Category | # of metabolite |
---|
br08003 Category | KEGG ID | KNApSAcK ID |
---|
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
O75496 | Geminin | Unclassified protein | C00001157 C00001164 C00001166 C00001168 C00001169 C00001172 C00040932 C00048928 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00001157 C00001166 C00001168 C00001169 C00001172 C00040932 C00048928 | 1 / 1 |
P10323 | Acrosin | S1A | C00001164 | 0 / 0 |
P02545 | Prelamin-A/C | Unclassified protein | C00001164 | 11 / 10 |
P16278 | Beta-galactosidase | Enzyme | C00001164 | 4 / 6 |
P06280 | Alpha-galactosidase A | Enzyme | C00001164 | 1 / 1 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00001164 | 0 / 0 |
O43451 | Maltase-glucoamylase, intestinal | Hydrolase | C00001164 | 0 / 0 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00001164 | 1 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#301500 | Fabry disease |
P06280
|
#230500 | Gm1-gangliosidosis, type i |
P16278
|
#230600 | Gm1-gangliosidosis, type ii |
P16278
|
#230650 | Gm1-gangliosidosis, type iii |
P16278
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#253010 | Mucopolysaccharidosis type ivb |
P16278
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
|
H00294 | Dilated cardiomyopathy (DCM) |
P02545
(related)
|
H00420 | Familial partial lipodystrophy (FPL) |
P02545
(related)
|
H00563 | Emery-Dreifuss muscular dystrophy |
P02545
(related)
|
H00590 | Congenital muscular dystrophies (CMD/MDC) |
P02545
(related)
|
H00593 | Limb-girdle muscular dystrophy (LGMD) |
P02545
(related)
|
H00601 | Hutchinson-Gilford progeria syndrome |
P02545
(related)
|
H00663 | Restrictive dermopathy |
P02545
(related)
|
H00665 | Mandibuloacral dysplasia |
P02545
(related)
|
H01216 | Left ventricular noncompaction (LVNC) |
P02545
(related)
|
H00125 | Fabry disease |
P06280
(related)
|
H00123 | Mucopolysaccharidosis type IV (MPS4) |
P16278
(related)
|
H00276 | Galactosialidosis |
P16278
(related)
|
H00281 | GM1 gangliosidosis |
P16278
(related)
|
H00421 | Mucopolysaccharidosis (MPS) |
P16278
(related)
|
H00422 | Glycoproteinoses |
P16278
(related)
|
H00426 | Defects in the degradation of ganglioside |
P16278
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
Q13148
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|